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通过多重、实时、一步法逆转录聚合酶链反应成功进行基因表达分析,无论扩增的靶标是什么。

Successful gene expression analysis by multiplex, real-time, one-step RT-PCR, irrespective of the targets amplified.

作者信息

Engel Holger, Kueppers Corinna, Koenig Margaretha, Loeffert Dirk

机构信息

QIAGEN GmbH, Hilden, Germany

出版信息

Biotechniques. 2007 Aug;43(2):230-1. doi: 10.2144/000112560.

Abstract

Multiplex, real-time, one-step RT-PCR enables simultaneous quantification of several transcripts in one reaction vessel. This saves time and conserves precious sample material when analyzing the expression of reference and target genes in a particular sample. However, intensive PCR optimization is often required (1). We show that success in multiplex, real-time, one-step RT-PCR can be achieved at the first attempt with the QuantiTect Multiplex RT-PCR Kit, regardless of the combination of genes analyzed. In each of the multiplex assays carried out, all targets were amplified with high efficiency, which is important for precise relative quantification of gene expression levels by the deltadeltaC(T) method.

摘要

多重实时一步法逆转录聚合酶链反应(Multiplex, real-time, one-step RT-PCR)能够在一个反应容器中同时对多个转录本进行定量。在分析特定样本中参考基因和靶基因的表达时,这既节省时间,又能保存珍贵的样本材料。然而,通常需要进行大量的聚合酶链反应(PCR)优化(1)。我们证明,无论所分析基因的组合如何,使用QuantiTect多重逆转录聚合酶链反应试剂盒(QuantiTect Multiplex RT-PCR Kit)首次尝试就能成功进行多重实时一步法逆转录聚合酶链反应。在进行的每一次多重分析中,所有靶标均高效扩增,这对于通过ΔΔC(T)方法精确相对定量基因表达水平至关重要。

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